EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS157-10690 
Organism
Homo sapiens 
Tissue/cell
PANC-1 
Coordinate
chr4:10115610-10117730 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6MA0463.2chr4:10116379-10116395CGGCTTTCTAGGAATC+6.87
KLF14MA0740.1chr4:10117609-10117623GAGGGGGCGTGGCG-6.28
KLF16MA0741.1chr4:10117611-10117622GGGGGCGTGGC-6.62
PBX1MA0070.1chr4:10116731-10116743GCATCAATCAAA+6.32
SP3MA0746.2chr4:10117610-10117623AGGGGGCGTGGCG-6.82
SP8MA0747.1chr4:10117610-10117622AGGGGGCGTGGC-6.92
SPICMA0687.1chr4:10117035-10117049TGCTTCCTGTTTTT-6
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_01734chr4:10115764-10118561Aorta
SE_02758chr4:10116522-10118498Astrocytes
SE_04459chr4:10115514-10118183Brain_Anterior_Caudate
SE_05471chr4:10116532-10119955Brain_Cingulate_Gyrus
SE_08364chr4:10116063-10118051Brain_Inferior_Temporal_Lobe
SE_09623chr4:10114621-10120741CD14
SE_12329chr4:10117297-10118067CD3
SE_14886chr4:10116769-10120864CD4_Memory_Primary_7pool
SE_16236chr4:10116827-10120999CD4_Naive_Primary_7pool
SE_17168chr4:10116550-10120562CD4p_CD225int_CD127p_Tmem
SE_17601chr4:10114889-10126849CD4p_CD25-_CD45RAp_Naive
SE_18041chr4:10114662-10121218CD4p_CD25-_CD45ROp_Memory
SE_18604chr4:10090926-10121361CD4p_CD25-_Il17-_PMAstim_Th
SE_19188chr4:10115095-10120578CD4p_CD25-_Il17p_PMAstim_Th17
SE_21402chr4:10116230-10120367CD8_Memory_7pool
SE_22779chr4:10115919-10118581CD8_primiary
SE_23672chr4:10116381-10120266Colon_Crypt_1
SE_24384chr4:10116641-10120117Colon_Crypt_2
SE_26123chr4:10116045-10120882Duodenum_Smooth_Muscle
SE_27018chr4:10116322-10121117Esophagus
SE_30028chr4:10116946-10118234Fetal_Muscle
SE_32010chr4:10116541-10120433Gastric
SE_37776chr4:10116140-10119896HSMMtube
SE_38833chr4:10115045-10120109HUVEC
SE_39084chr4:10116274-10118476IMR90
SE_41136chr4:10116270-10120034Left_Ventricle
SE_42597chr4:10116137-10118617Lung
SE_45147chr4:10116298-10118154NHLF
SE_48189chr4:10116071-10119846Psoas_Muscle
SE_48835chr4:10116297-10118603Right_Atrium
SE_50444chr4:10116206-10121732Sigmoid_Colon
SE_51167chr4:10114584-10120461Skeletal_Muscle
SE_52707chr4:10116274-10118625Small_Intestine
SE_55072chr4:10116777-10121661Stomach_Smooth_Muscle
SE_66345chr4:10117182-10117874Jurkat
SE_69074chr4:10116185-10118650H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr41011680110117310
Number: 1             
IDChromosomeStartEnd
GH04I010113chr41011499310115663
Enhancer Sequence
CCTGCATTCC AAACAGACCA TCATCCTTCC TGAACGGTCA TGCCAATTCA TGTCACTTTT 60
TTTTCCAAGA GTACTTTGCC CTAAAAAAAA TCGTACCCAC CTTTACTTGA GTACCCAGTC 120
CACCCATCCA ACTAACAAGA GACTCAGTGC CTGATCTACA TCCAGCCCAG GGAGGGCTAT 180
ATTAGTAGCA TCTCGTGCTG ACCTGGCATT GCAGAAACTT AAAAATAATT GAGAAGGGAA 240
ACAGGGTAAC CCCTGAGAAG AAAATGGCAA ACCACGGGGA AGGGGTAAGA ATACAGAGCT 300
CAGAAACAGG CAGAATGGGT TTCACAAGCT GGGAAATGCT TTCTGCAAAG GGGTGCCTGT 360
CCCTGAATGA CCACTCCATT AGAAGCAGCT CCAGTTACTG GCCTGCCTCA CCTTGCTAAG 420
TCTGACTCCT CTTTAGAGTA ACGGACCCAT GTGGGGTGGA AAGAGATGCT ACAGTTTAAG 480
AAGCTATCAC AGGGCCAGAT GCACAGCAGG TACTTTATGT GAGGCCCCCT CCCTGGAAGT 540
CAATGTGGAC TGCAACGACA GGGAAGGCCT GGTTAGGGGC AAAACGAAAT ATCCTACTGC 600
TCTGTATCCG AGGACGTGTT AGTGGATTTT ATTTGCCAAA CTACTAAATA TCTCTTTAGG 660
GTTGTCTCAA TTTTTATTTT CTCAAAAGCC TCAGGACCTG CCTTCGGAGA CTTCCAGATC 720
ATTACCATTA GATCCCTGGT GATTTTCTCC AGTTCTAAGC AAGGCCCTTC GGCTTTCTAG 780
GAATCTGTGT GACTAGCAAG TTGTTAGCAC CTTCAAAGCA CATTCACACC CGCCCACCCC 840
CTCATTTGAG GGGCCCAGCA ATCCAGGGCA GGTAGAGCTC TGTCTTCCAG CAGAGGAACA 900
GCAGCGACTG CCTGGGTTAA CGAGACAGAT GCGGGCAGAG CCAGCAGCTC TTCGGACCAA 960
GAGGCTTCTC CTTTCACAGA GAAGGAAACT GAGACCCAGA GACCCCTTCA TTCCCTCAGC 1020
CAGTTGCTGG CCTCCTGGAG GGCAAGTGTG TCCGATCAAC AGTCCCAACC TACCAAGGGA 1080
AATCAGGCTG ACTTTAAGTT GACAACCCTT GTATGCCTAT GGCATCAATC AAAACATACA 1140
TCTTTGTGCC AGCCGCCCCC ACTAAGCACA GCACAGGAGA AATCACCCAA TGGCCGGGCC 1200
GGCACCTCCA ACTCCCACCC CACCAATTCC ATCACTCAGG CTGAGGAAGG GAAAAGCAAA 1260
ATTTAAGCGT GTAACCCAGG AAGGGAGGGA GACTGACAGA CTGGGTCACC CCAACAATTA 1320
CAGAGGAATA ACATGAATTT GCAAGGATTT CCCAAGGAGC TGGCTCTAGA AGCCTTTTCA 1380
GCCTGGGTAC CGGAGGCTTG CAGAGAATGA TTCATGGGAA AACACTGCTT CCTGTTTTTG 1440
CTTTGGGGCT TAGATCCATG GTGGCAGATC TGGCTGGCCC AGAGGCCCGG GTGTTTTTCC 1500
GGGCTCTGCC ATACTGGAAG ACCAGGGTAT TAACAGCGAG TTAGCTGAGT GCCATTCCAT 1560
TCAGCAAGGG CTCAAAGTGC ACCAGGCACC GCTGGGCTTG AGGGACGCCA GCAGCTCATT 1620
CATTCCATCT GCCCAGCCAG CAGGCGAAGC GAGAGTGGTC ATCATCTCAT CATCTGTTTT 1680
ACAGACGAGA AAACTGGGGC TCAGAGATGC CCAAATCGCC AATCTTCTCA AGGTCACGCA 1740
GCGGCCGACC GGGTCAGTCT GATCCCTCAA ATCCGGAGCC CTTGCTTTTA AGGAATGAAC 1800
TAATCTAATC TCCCATCCAC GTACTAACCA GGCCTGACCG TGCTTAGCTT CCAAGATCAG 1860
AGGCGATCCG GCGCTTTCAG GGTGCTATGA CCGTAGACAG AAACGAACTA AGACTCAGTT 1920
TCCTCATCAA GAAGGAGCAG ACAAGGACCT GGGTGAATCT GAGGCCGGCT TCCGGGGCTC 1980
CGAGGTGTGG CTCCCGGTAG AGGGGGCGTG GCGCCCTCAC CCTCCCCGGG CCAATGGGCA 2040
GGAGGTGAGA AGTGGAGAGG AAGGCGAATT ATCCCATCCC AAGGTGGCTC CGGAGCAGAA 2100
CCGCGCCCGG GGTAGGGGGT 2120